✦ LIBER ✦

A STEREOSELECTIVE SYNTHESIS OF UNSATURATED PHOSPHONATES BY WITTIG-HORNER REACTIONS OF BISPHOSPHONYLMETHANE WITH 5-ARYL-(3-METHYL)-2E,4E-PENTADIENALS

✍ Scribed by Shi, De Qing; Chen, Ru Yu

Book ID: 126852831
Publisher: Taylor and Francis Group
Year: 2000
Tongue: English
Weight: 327 KB
Volume: 164
Category: Article
ISSN: 1042-6507
DOI: 10.1080/10426500008045248

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Convenient preparative method for synthe

Convenient preparative method for synthesis of methyl (Z)-3-aryl-2-(carbobenzoxyamino)acrylates by Wittig—Horner reaction with the use of Et3N as a base

✍ V. I. Tararov; T. F. Savel'eva; Yu. N. Belokon' 📂 Article 📅 1995 🏛 Springer 🌐 English ⚖ 290 KB

ChemInform Abstract: Convenient Preparat

ChemInform Abstract: Convenient Preparative Method for the Synthesis of Methyl (Z)-3-Aryl-2- (carbobenzoxyamino)acrylates by Wittig-Horner Reaction with the Use of NEt3 as a Base

✍ V. I. TARAROV; T. F. SAVEL'EVA; YU. N. BELOKON' 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

Oxazepines and thiazepines. 41 . Synthes

Oxazepines and thiazepines. 41 . Synthesis of 4-aryl-2,3-dihydro-2-styryl-1,5-benzothiazepines by the reaction of (E,E)-cinnamylideneacetophenones with 2-aminothiophenol and their conversion into 2,2-disubstituted 3-acetyl-2,3-dihydrobezothiazoles

✍ Albert Lévai 📂 Article 📅 2004 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 157 KB

## Abstract New 4‐aryl‐2,3‐dihydro‐2‐styryl‐1,5‐benzothiazepines **8–13** have been synthesized by an acid catalyzed reaction of 2‐arninothiophenol (**1**) and (__E,E__)‐cinnamylideneacetophenones **2–7.** Ring contraction of 1,5‐benzothiazepines **8–13** provided 2,2‐disubstituted 3‐acetyl‐2,3‐dih

Oxazepines and Thiazepines. Part 41. Syn

Oxazepines and Thiazepines. Part 41. Synthesis of 4-Aryl-2,3-dihydro-2-styryl-1,5-benzothiazepines by the Reaction of (E,E)-Cinnamylideneacetophenones with 2-Aminothiophenol and Their Conversion into 2,2-Disubstituted 3-Acetyl-2,3-dihydrobenzothiazoles.

✍ Albert Levai 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 16 KB 👁 1 views

A facile synthesis of 3,4-dienamides by

A facile synthesis of 3,4-dienamides by the reaction of propargyl alcohols with cyclic amide acetals, and their stereoselective rearrangement to 2(E),4(Z)-dienamides promoted with alumina. Total synthesis of isochavicine

✍ Tsuboi, Sadao; Nooda, Yuji; Takeda, Akira 📂 Article 📅 1984 🏛 American Chemical Society 🌐 English ⚖ 581 KB

Enantioselective synthesis of (3S,5R,6E,

Enantioselective synthesis of (3S,5R,6E,8E)-Deca-6,8-dien-1,3,5-triol, a new metabolite from Streptomyces Fimbriatus via asymmetric reaction of diketene with 2,4-hexadienal promoted by chiral Schiff base-titanium alkoxide complexes

✍ Masahiko Hayashi; Hiroko Kaneda; Nobuki Oguni 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 347 KB